US20050166569A1 - Low emission thermal plant - Google Patents
Low emission thermal plant Download PDFInfo
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- US20050166569A1 US20050166569A1 US10/499,872 US49987204A US2005166569A1 US 20050166569 A1 US20050166569 A1 US 20050166569A1 US 49987204 A US49987204 A US 49987204A US 2005166569 A1 US2005166569 A1 US 2005166569A1
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- 238000002485 combustion reaction Methods 0.000 claims abstract description 99
- 238000000034 method Methods 0.000 claims abstract description 33
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- 239000001301 oxygen Substances 0.000 claims abstract description 22
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 22
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- 238000010521 absorption reaction Methods 0.000 claims description 20
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Images
Classifications
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F01—MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
- F01K—STEAM ENGINE PLANTS; STEAM ACCUMULATORS; ENGINE PLANTS NOT OTHERWISE PROVIDED FOR; ENGINES USING SPECIAL WORKING FLUIDS OR CYCLES
- F01K23/00—Plants characterised by more than one engine delivering power external to the plant, the engines being driven by different fluids
- F01K23/02—Plants characterised by more than one engine delivering power external to the plant, the engines being driven by different fluids the engine cycles being thermally coupled
- F01K23/06—Plants characterised by more than one engine delivering power external to the plant, the engines being driven by different fluids the engine cycles being thermally coupled combustion heat from one cycle heating the fluid in another cycle
- F01K23/08—Plants characterised by more than one engine delivering power external to the plant, the engines being driven by different fluids the engine cycles being thermally coupled combustion heat from one cycle heating the fluid in another cycle with working fluid of one cycle heating the fluid in another cycle
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23J—REMOVAL OR TREATMENT OF COMBUSTION PRODUCTS OR COMBUSTION RESIDUES; FLUES
- F23J2215/00—Preventing emissions
- F23J2215/50—Carbon dioxide
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E20/00—Combustion technologies with mitigation potential
- Y02E20/32—Direct CO2 mitigation
Definitions
- the present invention relates to a method for regulation of the CO 2 content in combustion products from a pressurised, non-adiabatic combustion chamber before expansion of the products of combustion to atmospheric pressure, an installation for execution of the method and a thermal power plant where the present method is used.
- the concentration of CO 2 in the atmosphere has increased by nearly 30% in the last 150 years.
- the concentration of methane has doubled and the concentration of nitrogen oxides has increased by about 15%. This has increased the atmospheric greenhouse effect, something which has resulted in:
- Discharge gas from thermal power plants typically contains 4 to 10% by volume of CO 2 , where the lowest values are typical for gas turbines, while the highest values are only reached in combustion chambers with cooling, for example, in production of steam.
- Air separation By separating the air that goes into the combustion installation into oxygen and nitrogen, circulating CO 2 can be used as a propellant gas in a power plant. Without nitrogen to dilute the CO 2 formed, the CO 2 in the exhaust gas will have a relatively high partial pressure, approximately up to 1 bar. Excess CO 2 from the combustion can then be separated out relatively simply so that the installation for collection of CO 2 can be simplified. However the total costs for such a system becomes relatively high, as one must have a substantial plant for production of oxygen in addition to the power plant. Production and combustion of pure oxygen represent considerable safety challenges, in addition to great demands on the material. This will also most likely require development of new turbines.
- Hydrocarbon fuels are converted (reformed) to hydrogen and CO 2 in pressurised processing units called reformers.
- the product from the reformers contains CO 2 with a high partial pressure so that CO 2 can be separated out and deposited or used in another way.
- Hydrogen is used as fuel.
- the total plant becomes complicated and expensive, as it comprises a hydrogen-generating plant and a power plant.
- a common feature of the alternative methods for capture of CO 2 from a power plant is that they strive for a high partial pressure of CO 2 in the processing units where the cleaning is carried out.
- alternative methods are characterised by long-term, expensive and risky developments, with a typical time frame of 15 years research and a further 5 to 10 years or more before operating experience is attained. Expected electrical efficiency is up to 56 to 58% for a plant without cleaning and probably, somewhat optimistically, 45 to 50% with cleaning. An extended time frame is environmentally very undesirable.
- Partial pressure of oxygen down towards 0.2 bar where CO 2 shall be captured for thereby to minimise the degradation of the absorption agent.
- a method for the generation of electric power from a carbonaceous fuel in which the fuel is combusted in the presence of oxygen under elevated pressure in a combustion chamber.
- the exhaust gas from the combustion is separated into one CO 2 rich fraction which is treated so that it is not discharged to the environment, and one CO 2 depleted fraction which is expanded over one or more turbines for operation of other processes and/or generation of electric energy, before it is released into the surroundings, where the temperature in the combustion chamber is reduced under generation of steam which is expanded over steam turbines connected to an electricity generator for generation of electric power.
- Combustion under pressure in a combustion chamber as described above gives a considerable advantage in that a high partial pressure of CO 2 and a low partial pressure of oxygen in the combustion products are obtained without re-circulation of gas and without abnormally high temperatures of the combustion products.
- more than 50%, preferably more than 60% and most preferably more that 70%, such as for example above 80% of the heat energy from the combustion in the combustion chamber is taken out in the form of steam.
- critical units such as high temperature pressurised heat exchangers (above 600° C.) is reduced, and the use of such units is reduced to a minimum. This is achieved by a sizeable reduction of the load on such units.
- the exhaust gas from the combustion chamber is cooled by heat exchange with the CO 2 depleted fraction for heating of the CO 2 depleted fraction before this is expanded over turbines. This leads to increased efficiency in that the heat energy in the exhaust gas is taken care of and is used to drive the turbines.
- water and/or air is added to the cleaned CO 2 depleted fraction to increase the ability of the CO 2 depleted fraction to take up heat from the hot exhaust gas from the combustion chamber.
- the fuel is heated before it is fed to the combustion chamber. It has been found that this will increase the efficiency of the total process, i.e. that as much as possible of the chemical energy in the fuel is converted to electric energy.
- the fuel is heated in heat exchanging with a part stream from the air compressor and where the heat-exchanged, and thus cooled, compressed air stream is added to the CO 2 depleted fraction to increase its heat capacity.
- a thermal power plant for carbonaceous fuel preferably a hydrocarbon
- a thermal power plant for carbonaceous fuel comprising a combustion chamber in which the fuel is combusted under elevated pressure in the presence of oxygen, an exhaust gas line for leading of the combustion gas from the combustion chamber to a contact device where the exhaust gas is brought after cooling into contact with an absorption agent in which mainly CO 2 is absorbed and where the other gases in the exhaust gas, in the main, are not absorbed, a gas line ( 14 ) for the non-absorbed gas from the contact device, means to reheat the CO 2 depleted gas stream, means for expansion of this heated CO 2 depleted gas stream before it is released into the surroundings, and means to transport the absorption agent with absorbed CO 2 from the contact device to be deposited or to means for regeneration of the absorption agent for recycling to the contact device, where the combustion chamber comprises means to provide steam and lines to feed the steam to steam-turbines to expand.
- the thermal power plant comprises a condensation chamber for condensation of water in the exhaust gas arranged before the contact device. In this way water which arises from the combustion of the exhaust gas is removed. Water is unwanted in the cleaning process as it can harm/destroy the absorption agent.
- the thermal power plant comprises means to supply the water, which is condensed in the condensation chamber, to the CO 2 depleted fraction to increase the heat capacity of this fraction.
- the combustion chamber comprises an outer shell and an inner shell between which a cooling agent flows and where a pipe that covers the inner surface of the combustion chamber is arranged, and means to circulate water through the pipe.
- FIG. 1 is a simplified flow diagram that shows a basic embodiment of a gas power station according to the present invention
- FIG. 2 is an alternative embodiment with increased efficiency
- FIG. 3 is an embodiment of a pressurised combustion chamber where the outer shell is protected against the temperature of the combustion products with the aid of circulating CO 2 gas and circulating boiler water.
- the basic configuration, as illustrated in FIG. 1 will be described first.
- the flow diagram is independent of the size of the plant but, with respect to the amounts described here, refers to a 400 MW plant.
- the oxygen containing gas such as air, oxygen-enriched air or oxygen, hereafter referred to in the present description and patent claims as “air”, that enters the plant in an air line 1 , is compressed in a compressor 2 , 2 ′.
- the compressor can be in one stage, but it is preferred that the compressor 2 is two or more compressors in series, preferably with intermediate cooling of the air between the compressors 2 and 2 ′ as shown by a heat exchanger 45 that cools the air in line 3 ′ between the two compressors.
- Two compressors, 2,2′, as shown in FIG. 1 are preferred at the favoured working pressure for the present invention which lies around 16 bar.
- the incoming air is compressed in the compressor 2 ′ to around 4 bar.
- the air is led from compressor 2 ′ to compressor 2 by way of a line 3 ′.
- the air in the line 3 ′ is cooled in a heat exchanger 45 between the compressors before it is led into compressor 2 .
- compressor 2 the air is further compressed to a pressure of around 16.7 bar.
- the need for air to the combustion in such a plant is around 400 kg air/s.
- the compressed air is led by way of a line 3 to a combustion chamber 6 .
- the pressure of the air is adjusted to the working pressure in the combustion chamber so that the air is forced into the chamber.
- the pressure must lie above the working pressure in the combustion chamber by, for example 0.5 to 1 bar, such as 0.7 bar.
- Fuel containing carbon or carbon compounds, such as for example hydrocarbons such as gas or oil, are fed to the combustion chamber 6 through fuel supply 9 .
- Fuel that shall go into the combustion chamber 6 is pressurised by a pump (not shown) or the like to a pressure that permits the fuel to be forced into the combustion chamber.
- the pressure here must lie above the working pressure in the combustion chamber by, for example 0.5 to 1 bar, such as 0.7 bar.
- For use of natural gas around 19 kg gas/s is used in such a plant.
- the combustion in the combustion chamber 6 occurs at a pressure from atmospheric pressure to an overpressure, such as from 1.5 to 30 bar, for example from 5 to 25 bar, such as from 10 to 20 bar.
- a pressure of around 16 bar has been found to be particularly preferred from the demands of the subsequent cleaning and separation of CO 2 and operation experience from gas turbines and air compressors. It is a combustion at a pressure of around 16 bar which is used in the example presented here.
- Total heat of combustion is here around 900MW.
- the supply of oxygen-containing gas and fuel is controlled such that the exhaust gas from the combustion chamber has a residual content of oxygen from 1 to 10%, preferably from 1.5 to 6% and more preferably from 2-4%. This is considerably lower than in a gas turbine where the exhaust gas typically contains around 15% oxygen.
- water that is supplied through the water supply 4 is heated to produce steam which is fed to, by way of a steam outlet 5 , and expanded over a steam turbine 53 .
- the expanded steam from the turbine 53 is thereafter led by way of supply 4 ′ to the combustion chamber 6 to be heated up again.
- the re-heated steam leaves the combustion chamber in a line 5 ′ where it is led to a steam turbine 54 where it is expanded.
- the steam is led in a line 56 to a low-pressure turbine 57 where it is expanded further.
- the steam turbines 53 , 54 and the low-pressure turbine 57 are preferably arranged on a common shaft 55 that drives a generator 58 for generation of electric energy.
- a heat exchanger 62 which heat exchanges the cold stream in line 59 with a warmer stream in line 63 .
- the stream in line 63 is a stream which is taken from the low-pressure turbine at a point where the steam is not completely expanded.
- the stream in line 63 is again pumped up to desired pressure in the further circulation with the aid of a pump 64 .
- the streams in lines 59 and 63 are brought together in a line 65 which is heat exchanged with the exhaust gas from the combustion in an exhaust gas line 41 , in a heat exchanger 67 to take care of residual heat before the water is led into a water tank 66 .
- a part stream of the cooled water in line 59 can be taken out in a line 68 and heated up by heat exchange possibly initially with the partially cooled exhaust gas in line 41 in a heat exchanger 69 and thereafter with the hot air in line 3 ′ before the water in line 68 is led into the water tank 66 .
- the water is led by way of a line 70 to a pump 71 where the water is pumped to a desired pressure. From the pump 71 , the water is led in line 70 to a heat exchanger 17 where the water is heated up by heat exchange with the warm exhaust gas in line 41 . It may be desirable to take out smaller streams from the steam turbines 53 and 54 in lines 72 and 73 , respectively, and heat exchange these streams with a side stream of the stream in line 70 , shown with a line 76 , and use these for heating of the water. Heated water from the heat exchangers 17 and 74 , respectively, is led into line 4 and in for cooling of the combustion chamber.
- the gas in the combustion chamber 6 is cooled by this production of steam so that the working temperature in the combustion chamber is kept in the area 700 to 900° C., typically in the area 800 to 850° C.
- Preferably more than 50%, more preferred more than 60%, most preferred more than 70% of the heat energy from the combustion in the combustion chamber is taken out as hot steam in the cooling of the combustion chamber.
- the very large amount of heat which is removed from the combustion chamber ensures that most of the oxygen in the air can be used without the temperature becoming unacceptably high.
- the heat load on the critical gas-gas heat exchanger 8 is considerably reduced, something which gives reduced dimensions and simpler construction.
- the low temperature and reduced heat load also means that one has fewer problems with heat expansion and corrosion than at higher temperature and heat load. Plant costs and maintenance costs can thereby be reduced, at the same time as more energy is produced and cleaning of the exhaust gas is simplified without a great loss of electrical efficiency.
- the exhaust gas from the combustion chamber 6 is led through an exhaust gas pipe 10 , through one or more gas-gas heat exchangers 8 , 11 and a trim cooler 12 , where the exit gas is cooled before it is led into a contact device 13 where the gas is brought into contact with an absorption agent.
- the pressure in the contact device 13 lies close to the pressure in the combustion chamber 6 as the pressure is only reduced corresponding to the drop in pressure through the heat exchangers 8 , 11 and the trim cooler 12 .
- Water which is a result of the combustion in the combustion chamber 6 and which is condensed during the cooling of the exhaust gas through heat exchangers, is separated in a water separator 50 before the contact device 13 . Water can dilute and otherwise damage the absorption agent in the contact device.
- heat exchangers 8 , 11 are two heat exchangers that are connected in series.
- the number of heat exchangers and the dimensioning of these are dependent on the actual dimensioning and design of an actual plant and can therefore vary from plant to plant.
- a typical plant will contain from two to four heat exchangers in series.
- the temperature in the contact device 13 is dependent on the absorption agent and is a compromise between low temperature which gives high solubility, and higher temperature which promotes reactions associated with the absorption process. Typical temperatures are below 20° C. for water, 50° C. for amines and 80 to 100° C. for use of inorganic solutions, such as potassium carbonate.
- the preferred absorption agents are fluids such as water, an amine solution or an inorganic aqueous solution such as a carbonate solution which can absorb relatively large amounts of CO 2 at high pressure and high partial pressure of CO 2 .
- the absorption agent in the contact device 13 preferably runs down a large inner surface counter-current to the gas.
- the contact device is preferably operated at an elevated pressure, for example above 8 bar, more preferably above 10 bar.
- the pressure can also be higher such as for example above 15 or 20 bar.
- the gas from the exhaust gas which is not absorbed in the solvent is led from the contact device through a gas pipe 14 , through heat exchangers 11 , 8 where the gas is heated before it is expanded in turbine 15 , 15 ′ so that the energy is able to be used in the hot, high-pressure gas further on in the process.
- Water from the water separator 50 is preferably taken out through a line 52 , pumped by a pump 51 and led, together with the cleaned gas, into line 14 .
- the water is evaporated in the heating of the cleaned gas and supplies the gas with a part of the mass, which has been removed in the condensation of water and cleaning, and thus increases the heat capacity of the gas.
- the efficiency can also be increased by inserting a compressor in line 14 , between the contact device 13 and heat exchangers 11 , 8 .
- This compression heats the gas, a heat which can be taken out again later, and it makes it possible to permit a greater pressure drop in the heat exchangers.
- turbine 15 is more than one turbine, such as, for example two turbines, 15 and 15 ′, connected in series, where a line 14 ′ leads the gas which is partially expanded in turbine 15 to turbine 15 ′.
- compressor 2 ′ and turbine 15 ′ are arranged on a common shaft 40 ′ and that the compressor 2 ′ and the turbine 15 ′ are rated so that the kinetic energy from the turbine 15 ′ is just sufficient to drive the compressor 2 ′.
- Compressor 15 is arranged on a shaft 40 together with compressor 2 and a generator 16 .
- the kinetic energy from turbine 15 is greater than what is required to drive the compressor 2 and the remaining kinetic energy is therefore used to produce electricity in a generator 16 which is placed on the same shaft.
- the generator works as a motor in the start-up of the plant.
- This kinetic energy can, if required, naturally also be used for other purposes, such as for example a re-circulation pump for the absorption agent, a re-circulation pump for boiler water, a vacuum pump, a compressor for the enriched CO 2 , or a combination of these.
- the expanded exit gas from the turbine 15 is led through a heat exchanger 17 where the residual heat in the gas is used for a suitable application in the plant. In the embodiment shown, this heat is used to heat the water in line 4 .
- the solvent containing CO 2 is fed from the contact device 13 by way of a pipe 19 , by way of a heat exchanger 20 and an expansion device (not shown) inside a desorption device 18 .
- the pressure in the desorption device 18 is dependent on the choice of absorption agent, the amount of absorbed CO 2 and the demands for regeneration. The pressure will normally be lower than the pressure in the contact device 13 and will normally be between 0.2 and 1 bar above the surrounding pressure.
- a part of the absorbent will normally be removed in the bottom of the desorption device and be led through a circulation pipe 44 through a circulation heater 22 , where the absorbent is heated before it is led back to the desorption device 18 .
- Heat energy to the circulation heater 22 can be taken out from another location in the plant, for example, in that a stream of steam is taken out, at a suitable pressure and temperature, from the low-temperature turbine 57 and led in a line 76 to the heat exchanger 22 where the stream in the circulation pipe 44 is heated up by the hotter stream in line 76 .
- the steam that has been taken out in line 76 is condensed in the heat exchanger and is pumped further to a water tank 66 by a pump 77 .
- a pump 77 For example, 30 kg steam/s can be taken out in line 76 at a temperature of 200° C. and a pressure of 2.4 bar.
- CO 2 rich gas which is released in the desorption device 18 is removed from the top of this and is then preferably led through a condenser 23 , where it is cooled, and a liquid separator 24 , before it is led through a CO 2 pipe 25 as an CO 2 rich gas stream. Liquid which is separated out in the liquid separator 24 is returned to the desorption device through a liquid-carrying pipe 26 .
- Regenerated absorbent from the bottom of the desorption device 18 is removed and pumped through a re-circulation pipe 43 , cooled in a heat exchanger 20 , and possibly further heat exchangers, before it is returned to the absorption device 13 .
- the CO 2 rich gas stream from the liquid separator 24 is led to a compressor system 28 through a CO 2 -carrying pipe 25 , said compressor system comprises a number of compression steps in which the gas is compressed in such a way that it can be stored, transported, deposited in a secure way or be sold.
- This compressor system are of a conventional type and will not be described further here.
- This CO 2 rich gas stream will typically contain from around 80-95%, and preferably more than 90%, of the total CO 2 from the combustion according to the design and control parameters of the plant.
- the gas which is led out in pipe 14 from the contact device 13 has a low CO 2 content, typically around 10% of the total CO 2 from the combustion.
- this gas is supplied, through line 52 , with water that has previously been removed from the exhaust gas, it is heated by heat exchange with the hot exhaust gas in heat exchangers 11 and 8 before it is expanded over the turbines 15 , 15 ′.
- An essential feature of the present method and device is that a substantial part of the heat energy from the combustion in the combustion chamber 6 is taken out as steam which is used to drive the steam turbines 53 , 54 and 57 .
- a substantial part of the heat energy is taken out as steam, a feature which is much different from conventional solutions, the temperature in the combustion chamber and consequently of the exhaust gas from the combustion chamber is moderate and adapted to the operation of the gas turbine, and the combustion chamber pressure shell is further cooled, in spite of nearly full utilisation of the oxygen content of the air and thereby production of a high partial pressure of CO 2 .
- FIG. 1 of a plant according to the present invention can be varied with respect to heat exchangers, pumps, etc, without this diverting from the inventive concept.
- Elements that are shown here with a symbol can be a combination of similar or different elements which together give the desired and described function.
- a heat exchanger can describe a combination of heat exchangers, Likewise, such a plant will be able to encompass further elements which are not described here, such as further heat exchangers to take care of smaller amounts of energy, pumps or pressure reducing valves to regulate the pressure in certain elements, etc.
- a good increase in efficiency can be obtained by a combination in which the fuel gas is pre-heated, at the same time as additional amounts of cooled air are supplied to the cold side of heat exchanger 11 .
- Energy for heating of this gas can be taken out from different locations where cooling is required, or can be taken out from the compressors 2 , 2 ′ as shown in FIG. 2 .
- Some of the air for example, about 45 kg air/s, is taken from stream 3 .
- the additional amount of air is led in a line 7 , by way of a heat exchanger 80 , where it is heat exchanged with the incoming fuel gas in line 9 , 19 kg/s at 15° C., to heat the fuel gas up to around 240° C., while the air is cooled down to around 60° C.
- the cooled air in line 7 is led to line 14 where it is added to the exhaust gas to give a greater stream volume and greater mass to increase the ability of the gas to take up heat and thereby cool the exhaust gas in line 10 with the aid of heat exchangers 8 , 11 .
- This preheating as given in FIG. 2 can, according to calculations, give an increase of around 1% in the efficiency of the power plant for conversion of heat energy to electric power by combustion.
- line 7 can alternatively be supplied with air directly from the compressors 2 , 2 ′ or from a separate compressor (not shown).
- FIG. 3 shows such a combustion chamber 100 , comprising an outer shell 101 , an inner shell 102 , between which shells a cooling medium, such as for example CO 2 , can flow.
- CO 2 can be added through a cooling agent supply 106 .
- Heated CO 2 is taken out and circulated by way of a cooling circuit for CO 2 (not shown).
- the heat energy from the hot CO 2 is preferably added to streams in the process which have a need for heat, with the help of lines (not shown) to either some of the heat exchangers that are shown in FIGS. 1 and 2 or heat exchangers that are not shown.
- Fuel and oxygen containing gas such as clean gas, oxygen enriched air or air, are supplied through lines 9 and 3 , respectively, to one or more burners 103 .
- CO 2 can also be led further around pipe 107 for flue gas, from the combustion chamber to downstream heat exchangers, where it can also be used for cooling.
- the amount of CO 2 that circulates between the outer and inner shells is regulated so that the temperature of the outer shell 101 does not exceed 350° C., preferably does not exceed 300° C. With the temperature of the outer shell being kept below 350° C., one can use relatively inexpensive materials here and the production of this becomes simpler and cheaper than if the shell should withstand higher temperatures.
- an inner shell 102 is arranged, which is manufactured from a heat-resistant material. Preferentially, there is no pressure drop or only a small pressure drop between the inner and outer sides of the inner shell so that this is not exposed to large pressure loads.
- the wall of the combustion chamber can comprise more than two shells.
- the inner wall of the combustion chamber i.e. inside the inner wall 102
- the inner wall of the combustion chamber is covered by one or more pipes 104 that lie as one or more spirals along the wall.
- the spiral pipe 104 preferably covers the whole of the inner surface of the inner shell and protects this against combustion products inside the combustion chamber at the same time as it lowers the temperature both in the combustion chamber and of the inner wall 102 .
- the pipe 104 will lead a stream of boiler water which gives an extra safety against the temperature of the outer pressure-shell not exceeding 300 to 350° C.
- This heat which is added to the water in the pipes 104 can, for example, be added to the boiler water as preheating, in that the pressurising gas circulates by way of a heat exchanger where this heat is used for heating in lines where one has a need for heat at the relevant temperatures.
- the temperature in the combustion chamber is lowered further with heat spirals 105 , which is a combination of several heat spirals fitted inside the combustion chamber.
- the heat spirals 105 are heat spirals that are supplied with water/steam through lines 4 and 4 ′ and/or directly from the pipes 104 .
- a high-temperature heat exchanger should not be cooled down and heated up repeatedly if it shall also function as a pressure container. Therefore, it can be advantageous that hot heat exchangers, i.e. the heat exchangers in which one of the streams is above 350° C., is constructed with an outer pressure-shell and an inner shell between which flows a cooling medium, such as CO 2 or nitrogen, in the same way as for the combustion chamber.
- a cooling medium such as CO 2 or nitrogen
- the container around the heat exchanger can be cooled directly or indirectly with boiler water as the cooling agent.
- a further alternative is to build the heat exchanger inside the pressurised combustion chamber, where it does not need to function as a pressure container any longer.
- cooling gas such as CO 2
- heat exchanger 8 This heat energy in this cooling gas can be used in that it is supplied to heat exchangers for heating at locations in the process where it is possible to utilise low-grade energy, in particular this concerns preheating of water to the combustion chamber. Cooling of pressurised combustion chamber and pressurised heat exchangers to a shell temperature lower than 350 degrees C. gives the opportunity of using high tensile, low-alloy and inexpensive steel qualities.
- the system can also be used for heating of these elements before start-up of the plant. This reduces heat tensions and reduces the risk of cracking in pressure-shells and pipes.
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Abstract
Description
- The present invention relates to a method for regulation of the CO2 content in combustion products from a pressurised, non-adiabatic combustion chamber before expansion of the products of combustion to atmospheric pressure, an installation for execution of the method and a thermal power plant where the present method is used.
- The concentration of CO2 in the atmosphere has increased by nearly 30% in the last 150 years. The concentration of methane has doubled and the concentration of nitrogen oxides has increased by about 15%. This has increased the atmospheric greenhouse effect, something which has resulted in:
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- The mean temperature near the earth's surface has increased by about 0.5° C. over the last one hundred years, with an accelerating trend in the last ten years.
- Over the same period rainfall has increased by about 1%
- The sea level has increased by 15 to 20 cm due to melting of glaciers and because water expands when heated up.
- Increasing discharges of greenhouse gases is expected to give continued changes in the climate. Temperature can increase by as much as 0.6 to 2.5° C. over the coming 50 years. Within the scientific community, it is generally agreed that increasing use of fossil fuels, with exponentially increasing discharges of CO2, has altered the natural CO2 balance in nature and is therefore the direct reason for this development.
- It is important that action is taken immediately to stabilise the CO2 content of the atmosphere. This can be achieved if CO2 generated in a thermal power plant is collected and deposited safely. It is assumed that the collection represents three quarters of the total costs for the control of CO2 discharges to the atmosphere.
- Thus, an energy efficient, cost efficient, robust and simple method for removal of a substantial part of CO2 from the discharge gas will be desirable to ease this situation. It will be a great advantage if the method can be realised in the near future without long-term research.
- Discharge gas from thermal power plants typically contains 4 to 10% by volume of CO2, where the lowest values are typical for gas turbines, while the highest values are only reached in combustion chambers with cooling, for example, in production of steam.
- There are three opportunities for stabilising the CO2 content in the atmosphere. In addition to the capturing of CO2, non-polluting energy sources such as biomass can be used, or very efficient power plants can be developed. The capturing of CO2 is the most cost efficient. Still, relatively little development work is carried out to capture CO2, the methods presented up till now are characterised either by low efficiency or by a need for much long-term and expensive development. All methods for capturing CO2 comprise one or more of the following principles:
- Absorption of CO2. The exhaust gas from the combustion is brought into contact with an amine solution, at near atmospheric pressure. Some of the CO2 is absorbed in the amine solution which is then regenerated by heating. The main problem with this technology is that one operates with a low partial pressure of CO2, typically 0.04 bar, in the gas which shall be cleaned. The energy consumption becomes very high (about 3 times higher than if it is cleaned with a CO2 partial pressure of 1.5 bar). The cleaning plant becomes expensive and the degree of cleaning and size of the power plant are limiting factors. Therefore, the development work is concentrated on increasing the partial pressure of CO2. An alternative is that the exhaust gas is cooled down and re-circulated over the gas turbine. The effect of this is very limited due to the properties of the turbine, among other things. Another alternative is that the exhaust gas which is to be cooled down, is compressed, cooled down again, cleaned with, for example, an amine solution, heated up and expanded in a secondary gas turbine which drives the secondary compressor. In this way, the partial pressure of CO2 is raised, for example to 0.5 bar, and the cleaning becomes more efficient. An essential disadvantage is that the partial pressure of oxygen in the gas also becomes high, for example 1.5 bar, while amines typically degrade quickly at oxygen partial pressures above about 0.2 bar. In addition, costly extra equipment is required. Other combinations of primary and secondary power stations exist.
- Air separation. By separating the air that goes into the combustion installation into oxygen and nitrogen, circulating CO2 can be used as a propellant gas in a power plant. Without nitrogen to dilute the CO2 formed, the CO2 in the exhaust gas will have a relatively high partial pressure, approximately up to 1 bar. Excess CO2 from the combustion can then be separated out relatively simply so that the installation for collection of CO2 can be simplified. However the total costs for such a system becomes relatively high, as one must have a substantial plant for production of oxygen in addition to the power plant. Production and combustion of pure oxygen represent considerable safety challenges, in addition to great demands on the material. This will also most likely require development of new turbines.
- Conversion of the fuel. Hydrocarbon fuels are converted (reformed) to hydrogen and CO2 in pressurised processing units called reformers. The product from the reformers contains CO2 with a high partial pressure so that CO2 can be separated out and deposited or used in another way. Hydrogen is used as fuel. The total plant becomes complicated and expensive, as it comprises a hydrogen-generating plant and a power plant.
- A common feature of the alternative methods for capture of CO2 from a power plant is that they strive for a high partial pressure of CO2 in the processing units where the cleaning is carried out. In addition, alternative methods are characterised by long-term, expensive and risky developments, with a typical time frame of 15 years research and a further 5 to 10 years or more before operating experience is attained. Expected electrical efficiency is up to 56 to 58% for a plant without cleaning and probably, somewhat optimistically, 45 to 50% with cleaning. An extended time frame is environmentally very undesirable. In a United Nations Economic Commission for Europe (UNECE) conference in the autumn of 2002, “an urgent need to address the continuing exponential rise in global CO2 emissions” was emphasised and words such as “as soon as possible” and “need to go far beyond Kyoto protocol targets” were used.
- Thus there is a need for plants that overcome the mentioned problems, having the following characteristics:
- Realisable without long-term development, preferably with the use of rotary equipment that has already been tested out.
- Adapted for a sufficient partial pressure of CO2 so that conventional absorption installations can be used effectively, which means partial pressures up to 1.5 bar.
- Lowest possible gas stream volume where CO2 shall be captured.
- Partial pressure of oxygen down towards 0.2 bar where CO2 shall be captured for thereby to minimise the degradation of the absorption agent.
- Possibility for effective cleaning of NOx, which is typically carried out in the temperature range 300 to 400° C. Cleaning in a pressurised system is optimal.
- Efficiency in line with competing systems.
- Possibility for large installations above 400 MW.
- No use of secondary power systems, reformers, processes for production of oxygen or processes for conversion of the fuel.
- Compact and robust plant to benefit from the cost advantages by building the plant at shipyards on floating constructions. This also makes use at offshore installations possible.
- According to the present invention a method for the generation of electric power from a carbonaceous fuel is provided, in which the fuel is combusted in the presence of oxygen under elevated pressure in a combustion chamber. The exhaust gas from the combustion is separated into one CO2 rich fraction which is treated so that it is not discharged to the environment, and one CO2 depleted fraction which is expanded over one or more turbines for operation of other processes and/or generation of electric energy, before it is released into the surroundings, where the temperature in the combustion chamber is reduced under generation of steam which is expanded over steam turbines connected to an electricity generator for generation of electric power. Combustion under pressure in a combustion chamber as described above gives a considerable advantage in that a high partial pressure of CO2 and a low partial pressure of oxygen in the combustion products are obtained without re-circulation of gas and without abnormally high temperatures of the combustion products.
- It is preferred that more than 50%, preferably more than 60% and most preferably more that 70%, such as for example above 80% of the heat energy from the combustion in the combustion chamber is taken out in the form of steam. In that most of the energy is taken out as steam, the dependency of the efficiency on critical units, such as high temperature pressurised heat exchangers (above 600° C.) is reduced, and the use of such units is reduced to a minimum. This is achieved by a sizeable reduction of the load on such units.
- It is preferred that the exhaust gas from the combustion chamber is cooled by heat exchange with the CO2 depleted fraction for heating of the CO2 depleted fraction before this is expanded over turbines. This leads to increased efficiency in that the heat energy in the exhaust gas is taken care of and is used to drive the turbines.
- It is also preferred that water and/or air is added to the cleaned CO2 depleted fraction to increase the ability of the CO2 depleted fraction to take up heat from the hot exhaust gas from the combustion chamber.
- Similarly, it is preferred that the fuel is heated before it is fed to the combustion chamber. It has been found that this will increase the efficiency of the total process, i.e. that as much as possible of the chemical energy in the fuel is converted to electric energy.
- It is particularly preferred that the fuel is heated in heat exchanging with a part stream from the air compressor and where the heat-exchanged, and thus cooled, compressed air stream is added to the CO2 depleted fraction to increase its heat capacity.
- In combination with this, large amounts of “cheap” low-pressure steam are provided, i.e. without appreciably affecting the efficiency of the plant, for regeneration of the absorption agent. At the same time, the possibility of bringing back much of this low-grade energy arises, together with low-grade energy from the coolers in the compression train for CO2, as a useful contribution to the production of electric power. A further detail to collect low-grade energy for the energy production is included in that the use of a pressurised air-water mixture, at a suitable location in the plant, can give evaporation of water and thereby take up much energy at temperatures far below the boiling point for water at the prevailing pressure.
- It is a combination of these characteristics that makes it practically possible to realise the plant, with a competitive efficiency in the area of 43.5 to 46% or more dependent on the extent of optimisation and degree of cleaning of CO2. A degree of cleaning of 90% or more should be attainable.
- Furthermore, a thermal power plant for carbonaceous fuel, preferably a hydrocarbon, is described, comprising a combustion chamber in which the fuel is combusted under elevated pressure in the presence of oxygen, an exhaust gas line for leading of the combustion gas from the combustion chamber to a contact device where the exhaust gas is brought after cooling into contact with an absorption agent in which mainly CO2 is absorbed and where the other gases in the exhaust gas, in the main, are not absorbed, a gas line (14) for the non-absorbed gas from the contact device, means to reheat the CO2 depleted gas stream, means for expansion of this heated CO2 depleted gas stream before it is released into the surroundings, and means to transport the absorption agent with absorbed CO2 from the contact device to be deposited or to means for regeneration of the absorption agent for recycling to the contact device, where the combustion chamber comprises means to provide steam and lines to feed the steam to steam-turbines to expand.
- It is preferred that the thermal power plant comprises a condensation chamber for condensation of water in the exhaust gas arranged before the contact device. In this way water which arises from the combustion of the exhaust gas is removed. Water is unwanted in the cleaning process as it can harm/destroy the absorption agent.
- It is furthermore preferred that the thermal power plant comprises means to supply the water, which is condensed in the condensation chamber, to the CO2 depleted fraction to increase the heat capacity of this fraction.
- It is also preferred that the combustion chamber comprises an outer shell and an inner shell between which a cooling agent flows and where a pipe that covers the inner surface of the combustion chamber is arranged, and means to circulate water through the pipe.
- The present invention will now be explained in more detail with reference to preferred embodiments and the enclosed figures, in which:
-
FIG. 1 is a simplified flow diagram that shows a basic embodiment of a gas power station according to the present invention; -
FIG. 2 is an alternative embodiment with increased efficiency; -
FIG. 3 is an embodiment of a pressurised combustion chamber where the outer shell is protected against the temperature of the combustion products with the aid of circulating CO2 gas and circulating boiler water. - The basic configuration, as illustrated in
FIG. 1 , will be described first. The flow diagram is independent of the size of the plant but, with respect to the amounts described here, refers to a 400 MW plant. - The oxygen containing gas, such as air, oxygen-enriched air or oxygen, hereafter referred to in the present description and patent claims as “air”, that enters the plant in an
air line 1, is compressed in acompressor compressor 2 is two or more compressors in series, preferably with intermediate cooling of the air between thecompressors heat exchanger 45 that cools the air inline 3′ between the two compressors. Two compressors, 2,2′, as shown inFIG. 1 , are preferred at the favoured working pressure for the present invention which lies around 16 bar. The incoming air is compressed in thecompressor 2′ to around 4 bar. The air is led fromcompressor 2′ tocompressor 2 by way of aline 3′. The air in theline 3′ is cooled in aheat exchanger 45 between the compressors before it is led intocompressor 2. Incompressor 2 the air is further compressed to a pressure of around 16.7 bar. The need for air to the combustion in such a plant is around 400 kg air/s. - From
compressor 2 the compressed air is led by way of aline 3 to acombustion chamber 6. The pressure of the air is adjusted to the working pressure in the combustion chamber so that the air is forced into the chamber. Here, the pressure must lie above the working pressure in the combustion chamber by, for example 0.5 to 1 bar, such as 0.7 bar. - Fuel containing carbon or carbon compounds, such as for example hydrocarbons such as gas or oil, are fed to the
combustion chamber 6 throughfuel supply 9. Fuel that shall go into thecombustion chamber 6 is pressurised by a pump (not shown) or the like to a pressure that permits the fuel to be forced into the combustion chamber. Thus, the pressure here must lie above the working pressure in the combustion chamber by, for example 0.5 to 1 bar, such as 0.7 bar. For use of natural gas, around 19 kg gas/s is used in such a plant. - Use of burners that give a low NOx content in the exhaust gas are preferred due to the environmentally alarming aspects of releasing such gases. With the use of such burners, NOx from a boiler with low NOx burners will be reduced to below 50 ppm. According to known and tested technology, further NOx can be removed with NH3 (3NO+2NH3=2.5 N2+3H2O) in a cleaning unit (not shown). This cleaning has up to 90% efficiency at atmospheric pressure, but is assumed to be much better at 16 bar. It will therefore be possible to clean down to 5 ppm. By adapting the heat exchangers, the gas can be given a temperature that is optimal for this process. Other methods without NH3 also exist, methods which are relevant as NH3 gives some NH3 “slip”.
- The combustion in the
combustion chamber 6 occurs at a pressure from atmospheric pressure to an overpressure, such as from 1.5 to 30 bar, for example from 5 to 25 bar, such as from 10 to 20 bar. A pressure of around 16 bar has been found to be particularly preferred from the demands of the subsequent cleaning and separation of CO2 and operation experience from gas turbines and air compressors. It is a combustion at a pressure of around 16 bar which is used in the example presented here. - Total heat of combustion is here around 900MW.
- The supply of oxygen-containing gas and fuel is controlled such that the exhaust gas from the combustion chamber has a residual content of oxygen from 1 to 10%, preferably from 1.5 to 6% and more preferably from 2-4%. This is considerably lower than in a gas turbine where the exhaust gas typically contains around 15% oxygen.
- In the combustion, water that is supplied through the
water supply 4 is heated to produce steam which is fed to, by way of asteam outlet 5, and expanded over asteam turbine 53. The expanded steam from theturbine 53 is thereafter led by way ofsupply 4′ to thecombustion chamber 6 to be heated up again. The re-heated steam leaves the combustion chamber in aline 5′ where it is led to asteam turbine 54 where it is expanded. - From the
steam turbine 54, the steam is led in aline 56 to a low-pressure turbine 57 where it is expanded further. Thesteam turbines pressure turbine 57 are preferably arranged on acommon shaft 55 that drives agenerator 58 for generation of electric energy. - Most of the expanded steam/condensed water is led from the low-
pressure turbine 57 by way of aline 59 to aheat exchanger 60 which cools the water further with external cooling water. After cooling/complete condensation, the water inline 59 is pumped up to the desired pressure for further circulation with the aid of apump 61. This relatively cold water can be used to take care of low temperature energy at various locations in the plant in that it is heat exchanged with warmer streams which are to be cooled. This makes it possible to utilise/take care of low temperature heat energy, something which is essential for good energy economics. - This is illustrated here by a
heat exchanger 62 which heat exchanges the cold stream inline 59 with a warmer stream inline 63. The stream inline 63 is a stream which is taken from the low-pressure turbine at a point where the steam is not completely expanded. The stream inline 63 is again pumped up to desired pressure in the further circulation with the aid of apump 64. The streams inlines line 65 which is heat exchanged with the exhaust gas from the combustion in anexhaust gas line 41, in aheat exchanger 67 to take care of residual heat before the water is led into awater tank 66. - A part stream of the cooled water in
line 59 can be taken out in aline 68 and heated up by heat exchange possibly initially with the partially cooled exhaust gas inline 41 in aheat exchanger 69 and thereafter with the hot air inline 3′ before the water inline 68 is led into thewater tank 66. - From the
water tank 66 the water is led by way of aline 70 to apump 71 where the water is pumped to a desired pressure. From thepump 71, the water is led inline 70 to aheat exchanger 17 where the water is heated up by heat exchange with the warm exhaust gas inline 41. It may be desirable to take out smaller streams from thesteam turbines lines line 70, shown with aline 76, and use these for heating of the water. Heated water from theheat exchangers line 4 and in for cooling of the combustion chamber. - The gas in the
combustion chamber 6 is cooled by this production of steam so that the working temperature in the combustion chamber is kept in the area 700 to 900° C., typically in the area 800 to 850° C. Preferably more than 50%, more preferred more than 60%, most preferred more than 70% of the heat energy from the combustion in the combustion chamber is taken out as hot steam in the cooling of the combustion chamber. - The very large amount of heat which is removed from the combustion chamber ensures that most of the oxygen in the air can be used without the temperature becoming unacceptably high. This gives a high concentration of CO2 in the exhaust gas, consumption of relatively small amounts of air in relation to the amount of energy which is produced, and thereby the essential advantage that a relatively small volume stream of exhaust gas will have to be cleaned. When most of the electric energy is produced in efficient steam turbines, the heat load on the critical gas-
gas heat exchanger 8 is considerably reduced, something which gives reduced dimensions and simpler construction. The low temperature and reduced heat load also means that one has fewer problems with heat expansion and corrosion than at higher temperature and heat load. Plant costs and maintenance costs can thereby be reduced, at the same time as more energy is produced and cleaning of the exhaust gas is simplified without a great loss of electrical efficiency. - With reference to
FIG. 1 the exhaust gas from thecombustion chamber 6 is led through anexhaust gas pipe 10, through one or more gas-gas heat exchangers trim cooler 12, where the exit gas is cooled before it is led into acontact device 13 where the gas is brought into contact with an absorption agent. The pressure in thecontact device 13 lies close to the pressure in thecombustion chamber 6 as the pressure is only reduced corresponding to the drop in pressure through theheat exchangers trim cooler 12. - Water, which is a result of the combustion in the
combustion chamber 6 and which is condensed during the cooling of the exhaust gas through heat exchangers, is separated in awater separator 50 before thecontact device 13. Water can dilute and otherwise damage the absorption agent in the contact device. - In the enclosed figure,
heat exchangers contact device 13 is dependent on the absorption agent and is a compromise between low temperature which gives high solubility, and higher temperature which promotes reactions associated with the absorption process. Typical temperatures are below 20° C. for water, 50° C. for amines and 80 to 100° C. for use of inorganic solutions, such as potassium carbonate. - The preferred absorption agents are fluids such as water, an amine solution or an inorganic aqueous solution such as a carbonate solution which can absorb relatively large amounts of CO2 at high pressure and high partial pressure of CO2. The absorption agent in the
contact device 13 preferably runs down a large inner surface counter-current to the gas. - The contact device is preferably operated at an elevated pressure, for example above 8 bar, more preferably above 10 bar. The pressure can also be higher such as for example above 15 or 20 bar.
- The gas from the exhaust gas which is not absorbed in the solvent is led from the contact device through a
gas pipe 14, throughheat exchangers turbine water separator 50 is preferably taken out through aline 52, pumped by apump 51 and led, together with the cleaned gas, intoline 14. The water is evaporated in the heating of the cleaned gas and supplies the gas with a part of the mass, which has been removed in the condensation of water and cleaning, and thus increases the heat capacity of the gas. - The efficiency can also be increased by inserting a compressor in
line 14, between thecontact device 13 andheat exchangers - It can also be relevant to compensate for reduced mass flow because of the CO2 which is removed, by feeding in a small compressed gas stream which is taken out of
line 3, cool this gas down so that heat is not lost, for example by pre-heating thecombustion gas 9, which is shown inFIG. 2 , and lead this into the cleaned gas before theheat exchanger 11. It is preferred that the gas has about the same temperature as the gas inline 14 and cooling should therefore be rated according to this. - It is preferred that
turbine 15 is more than one turbine, such as, for example two turbines, 15 and 15′, connected in series, where aline 14′ leads the gas which is partially expanded inturbine 15 toturbine 15′. - It can be preferable that
compressor 2′ andturbine 15′ are arranged on acommon shaft 40′ and that thecompressor 2′ and theturbine 15′ are rated so that the kinetic energy from theturbine 15′ is just sufficient to drive thecompressor 2′.Compressor 15 is arranged on ashaft 40 together withcompressor 2 and agenerator 16. The kinetic energy fromturbine 15 is greater than what is required to drive thecompressor 2 and the remaining kinetic energy is therefore used to produce electricity in agenerator 16 which is placed on the same shaft. The generator works as a motor in the start-up of the plant. This kinetic energy can, if required, naturally also be used for other purposes, such as for example a re-circulation pump for the absorption agent, a re-circulation pump for boiler water, a vacuum pump, a compressor for the enriched CO2, or a combination of these. - From
turbine 15, the expanded exit gas from theturbine 15 is led through aheat exchanger 17 where the residual heat in the gas is used for a suitable application in the plant. In the embodiment shown, this heat is used to heat the water inline 4. - In the shown device, the solvent containing CO2 is fed from the
contact device 13 by way of apipe 19, by way of aheat exchanger 20 and an expansion device (not shown) inside adesorption device 18. The pressure in thedesorption device 18 is dependent on the choice of absorption agent, the amount of absorbed CO2 and the demands for regeneration. The pressure will normally be lower than the pressure in thecontact device 13 and will normally be between 0.2 and 1 bar above the surrounding pressure. - To increase the release of absorbed gas from the absorbent in the desorption device, a part of the absorbent will normally be removed in the bottom of the desorption device and be led through a circulation pipe 44 through a
circulation heater 22, where the absorbent is heated before it is led back to thedesorption device 18. Heat energy to thecirculation heater 22 can be taken out from another location in the plant, for example, in that a stream of steam is taken out, at a suitable pressure and temperature, from the low-temperature turbine 57 and led in aline 76 to theheat exchanger 22 where the stream in the circulation pipe 44 is heated up by the hotter stream inline 76. The steam that has been taken out inline 76 is condensed in the heat exchanger and is pumped further to awater tank 66 by a pump 77. For example, 30 kg steam/s can be taken out inline 76 at a temperature of 200° C. and a pressure of 2.4 bar. - The energy requirement for this circulation heater is minimised as the
contact device 13 is driven at a high partial pressure of CO2 in the incoming gas. At the same time, the steam which is used has a low value as it is already partly expanded over high-pressure and intermediate-pressure turbines - CO2 rich gas which is released in the
desorption device 18 is removed from the top of this and is then preferably led through acondenser 23, where it is cooled, and aliquid separator 24, before it is led through a CO2 pipe 25 as an CO2 rich gas stream. Liquid which is separated out in theliquid separator 24 is returned to the desorption device through a liquid-carryingpipe 26. - Regenerated absorbent from the bottom of the
desorption device 18 is removed and pumped through are-circulation pipe 43, cooled in aheat exchanger 20, and possibly further heat exchangers, before it is returned to theabsorption device 13. - The CO2 rich gas stream from the
liquid separator 24 is led to acompressor system 28 through a CO2-carrying pipe 25, said compressor system comprises a number of compression steps in which the gas is compressed in such a way that it can be stored, transported, deposited in a secure way or be sold. The components and construction of this compressor system are of a conventional type and will not be described further here. This CO2 rich gas stream will typically contain from around 80-95%, and preferably more than 90%, of the total CO2 from the combustion according to the design and control parameters of the plant. - The gas which is led out in
pipe 14 from thecontact device 13 has a low CO2 content, typically around 10% of the total CO2 from the combustion. As mentioned above, this gas is supplied, throughline 52, with water that has previously been removed from the exhaust gas, it is heated by heat exchange with the hot exhaust gas inheat exchangers turbines - An essential feature of the present method and device is that a substantial part of the heat energy from the combustion in the
combustion chamber 6 is taken out as steam which is used to drive thesteam turbines heat exchanger 8, which would be a weak part in a plant where most of the heat energy is taken out in gas turbines driven by the exhaust gas from the combustion. This is illustrated here by table 1, which gives a few important measuring values for a plant according to the present invention. - The configuration according to
FIG. 1 of a plant according to the present invention can be varied with respect to heat exchangers, pumps, etc, without this diverting from the inventive concept. Elements that are shown here with a symbol can be a combination of similar or different elements which together give the desired and described function. Thus, what has been illustrated as a heat exchanger can describe a combination of heat exchangers, Likewise, such a plant will be able to encompass further elements which are not described here, such as further heat exchangers to take care of smaller amounts of energy, pumps or pressure reducing valves to regulate the pressure in certain elements, etc. - Similarly, during the engineering and optimisation of a particular plant, one will be able to deviate from details in the described mass and energy flow.
- A good increase in efficiency can be obtained by a combination in which the fuel gas is pre-heated, at the same time as additional amounts of cooled air are supplied to the cold side of
heat exchanger 11. Energy for heating of this gas can be taken out from different locations where cooling is required, or can be taken out from thecompressors FIG. 2 . Some of the air, for example, about 45 kg air/s, is taken fromstream 3. The additional amount of air is led in aline 7, by way of aheat exchanger 80, where it is heat exchanged with the incoming fuel gas inline line 7 is led toline 14 where it is added to the exhaust gas to give a greater stream volume and greater mass to increase the ability of the gas to take up heat and thereby cool the exhaust gas inline 10 with the aid ofheat exchangers FIG. 2 can, according to calculations, give an increase of around 1% in the efficiency of the power plant for conversion of heat energy to electric power by combustion. - If one has no use for the heat in the compressed air for heat exchange with the fuel,
line 7 can alternatively be supplied with air directly from thecompressors - High temperatures and pressures place great demands on the construction and choice of materials for the hot components. Building of components, such as a combustion chamber and heat exchangers for high pressure and high temperature, is complicated and costly. A traditional combustion chamber for the pressure preferred here necessitates costly materials being chosen. It will be possible to reduce construction costs and vulnerability of the combustion chamber by the wall in the combustion chamber comprising two or more shells outside each other where the outer shell is a pressure shell and where the temperature of the outer shell can be kept below 350° C., preferably below 300° C.
-
FIG. 3 shows such acombustion chamber 100, comprising anouter shell 101, aninner shell 102, between which shells a cooling medium, such as for example CO2, can flow. CO2 can be added through acooling agent supply 106. Heated CO2 is taken out and circulated by way of a cooling circuit for CO2 (not shown). The heat energy from the hot CO2 is preferably added to streams in the process which have a need for heat, with the help of lines (not shown) to either some of the heat exchangers that are shown inFIGS. 1 and 2 or heat exchangers that are not shown. - Fuel and oxygen containing gas, such as clean gas, oxygen enriched air or air, are supplied through
lines more burners 103. - As shown in
FIG. 3 , CO2 can also be led further aroundpipe 107 for flue gas, from the combustion chamber to downstream heat exchangers, where it can also be used for cooling. The amount of CO2 that circulates between the outer and inner shells is regulated so that the temperature of theouter shell 101 does not exceed 350° C., preferably does not exceed 300° C. With the temperature of the outer shell being kept below 350° C., one can use relatively inexpensive materials here and the production of this becomes simpler and cheaper than if the shell should withstand higher temperatures. - Inside the
outer shell 101, aninner shell 102 is arranged, which is manufactured from a heat-resistant material. Preferentially, there is no pressure drop or only a small pressure drop between the inner and outer sides of the inner shell so that this is not exposed to large pressure loads. If desired, the wall of the combustion chamber can comprise more than two shells. - The inner wall of the combustion chamber, i.e. inside the
inner wall 102, is covered by one ormore pipes 104 that lie as one or more spirals along the wall. Thespiral pipe 104 preferably covers the whole of the inner surface of the inner shell and protects this against combustion products inside the combustion chamber at the same time as it lowers the temperature both in the combustion chamber and of theinner wall 102. Thepipe 104 will lead a stream of boiler water which gives an extra safety against the temperature of the outer pressure-shell not exceeding 300 to 350° C. This heat, which is added to the water in thepipes 104 can, for example, be added to the boiler water as preheating, in that the pressurising gas circulates by way of a heat exchanger where this heat is used for heating in lines where one has a need for heat at the relevant temperatures. - The temperature in the combustion chamber is lowered further with heat spirals 105, which is a combination of several heat spirals fitted inside the combustion chamber. The heat spirals 105 are heat spirals that are supplied with water/steam through
lines pipes 104. - A high-temperature heat exchanger should not be cooled down and heated up repeatedly if it shall also function as a pressure container. Therefore, it can be advantageous that hot heat exchangers, i.e. the heat exchangers in which one of the streams is above 350° C., is constructed with an outer pressure-shell and an inner shell between which flows a cooling medium, such as CO2 or nitrogen, in the same way as for the combustion chamber. Alternatively, the container around the heat exchanger can be cooled directly or indirectly with boiler water as the cooling agent. A further alternative is to build the heat exchanger inside the pressurised combustion chamber, where it does not need to function as a pressure container any longer.
- It can also be relevant to carry out other specific construction adjustments on some elements, in particular to improve operating safety, reduce building costs and reduce the danger of wear and associated errors. Thus, it can be relevant to use a cooling gas such as CO2 to cool the shell of the
combustion chamber 6 and other hot elements such as hot heat exchangers, forexample heat exchanger 8. This heat energy in this cooling gas can be used in that it is supplied to heat exchangers for heating at locations in the process where it is possible to utilise low-grade energy, in particular this concerns preheating of water to the combustion chamber. Cooling of pressurised combustion chamber and pressurised heat exchangers to a shell temperature lower than 350 degrees C. gives the opportunity of using high tensile, low-alloy and inexpensive steel qualities. The system can also be used for heating of these elements before start-up of the plant. This reduces heat tensions and reduces the risk of cracking in pressure-shells and pipes.
Claims (10)
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NO20023050A NO20023050L (en) | 2002-06-21 | 2002-06-21 | Process and facilities for carrying out the process |
NO20023050 | 2002-06-21 | ||
PCT/NO2003/000210 WO2004001301A2 (en) | 2002-06-21 | 2003-06-20 | Low emission thermal plant |
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US7328581B2 US7328581B2 (en) | 2008-02-12 |
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US10/499,872 Expired - Lifetime US7328581B2 (en) | 2002-06-21 | 2003-06-20 | Low emission thermal plant |
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US (1) | US7328581B2 (en) |
EP (1) | EP1539330A2 (en) |
JP (1) | JP4885449B2 (en) |
CN (1) | CN1317052C (en) |
AU (1) | AU2003278026A1 (en) |
CA (1) | CA2490429C (en) |
NO (1) | NO20023050L (en) |
RU (1) | RU2315186C2 (en) |
WO (1) | WO2004001301A2 (en) |
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Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4498289A (en) * | 1982-12-27 | 1985-02-12 | Ian Osgerby | Carbon dioxide power cycle |
US6637183B2 (en) * | 2000-05-12 | 2003-10-28 | Clean Energy Systems, Inc. | Semi-closed brayton cycle gas turbine power systems |
US7089743B2 (en) * | 1998-02-25 | 2006-08-15 | Alstom | Method for operating a power plant by means of a CO2 process |
Family Cites Families (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL7702650A (en) | 1977-03-11 | 1978-09-13 | Shell Int Research | PROCESS FOR THE REGENERATION OF AN ALKANOLAMINE-BASED SOLVENT FOR GASES CONTAINING CO2 AND / OR COS. |
JPH04350303A (en) * | 1991-05-27 | 1992-12-04 | Jgc Corp | Carbon dioxide gas recovery type thermal power generation system |
JP2565437B2 (en) * | 1991-09-03 | 1996-12-18 | 株式会社ヒラカワガイダム | Gas turbine device equipped with tube nest combustion type combustor |
EP0733395B1 (en) | 1991-10-09 | 2004-01-21 | The Kansai Electric Power Co., Inc. | Recovery of carbon dioxide from combustion exhaust gas |
JP2792777B2 (en) * | 1992-01-17 | 1998-09-03 | 関西電力株式会社 | Method for removing carbon dioxide from flue gas |
JP2871273B2 (en) * | 1992-03-26 | 1999-03-17 | 三菱重工業株式会社 | Carbon dioxide removal combustion device |
JPH0626362A (en) * | 1992-07-09 | 1994-02-01 | Mitsubishi Heavy Ind Ltd | Co2 gas turbine cycle |
NO180520C (en) * | 1994-02-15 | 1997-05-07 | Kvaerner Asa | Method of Removing Carbon Dioxide from Combustion Gases |
AU3276397A (en) * | 1996-06-28 | 1998-01-21 | Hiroyasu Tanigawa | Combined steam and gas turbine engine |
JP3782567B2 (en) * | 1997-12-10 | 2006-06-07 | 株式会社東芝 | Thermal power plant |
JPH11210493A (en) * | 1998-01-26 | 1999-08-03 | Toshiba Corp | Gas turbine plant |
JPH11264325A (en) * | 1998-03-18 | 1999-09-28 | Toshiba Corp | Carbon dioxide recovery type power generation plant |
AU744197B2 (en) | 1998-07-13 | 2002-02-21 | Statoil Asa | Process for generating electric energy, steam and carbon dioxide from hydrocarbon feedstock |
NO990812L (en) | 1999-02-19 | 2000-08-21 | Norsk Hydro As | Method for removing and recovering CO2 from exhaust gas |
NO993704D0 (en) * | 1999-03-26 | 1999-07-29 | Christensen Process Consulting | Procedure for controlling the CO2 content of an exhaust gas from a combustion chamber |
JP2000337108A (en) * | 1999-05-27 | 2000-12-05 | Mitsubishi Heavy Ind Ltd | Carbon dioxide recovery type combined generating system |
JP2001271610A (en) * | 2000-03-24 | 2001-10-05 | Toshiba Corp | Co2 recovery gas turbine system |
JP2002079052A (en) * | 2000-09-08 | 2002-03-19 | Toshiba Corp | Method and system for recovering carbon dioxide |
JP3969949B2 (en) * | 2000-10-25 | 2007-09-05 | 関西電力株式会社 | Amine recovery method and apparatus, and decarbonation gas apparatus provided with the same |
-
2002
- 2002-06-21 NO NO20023050A patent/NO20023050L/en not_active Application Discontinuation
-
2003
- 2003-06-20 WO PCT/NO2003/000210 patent/WO2004001301A2/en active Application Filing
- 2003-06-20 RU RU2005101350/06A patent/RU2315186C2/en not_active IP Right Cessation
- 2003-06-20 AU AU2003278026A patent/AU2003278026A1/en not_active Abandoned
- 2003-06-20 JP JP2004515248A patent/JP4885449B2/en not_active Expired - Fee Related
- 2003-06-20 CN CNB038175002A patent/CN1317052C/en not_active Expired - Fee Related
- 2003-06-20 US US10/499,872 patent/US7328581B2/en not_active Expired - Lifetime
- 2003-06-20 EP EP03756764A patent/EP1539330A2/en not_active Ceased
- 2003-06-20 CA CA2490429A patent/CA2490429C/en not_active Expired - Fee Related
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4498289A (en) * | 1982-12-27 | 1985-02-12 | Ian Osgerby | Carbon dioxide power cycle |
US7089743B2 (en) * | 1998-02-25 | 2006-08-15 | Alstom | Method for operating a power plant by means of a CO2 process |
US6637183B2 (en) * | 2000-05-12 | 2003-10-28 | Clean Energy Systems, Inc. | Semi-closed brayton cycle gas turbine power systems |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2007094675A1 (en) * | 2006-01-13 | 2007-08-23 | Co2-Norway As | Method and plant for removing carbon dioxide from flue gas |
GB2449578A (en) * | 2006-01-13 | 2008-11-26 | Co2 Norway As | Method and plant for removing carbon dioxide from flue gas |
US20090317315A1 (en) * | 2006-01-13 | 2009-12-24 | Co2-Norway As | Method and Plant for Removing Carbon Dioxide From Flue Gas |
GB2449578B (en) * | 2006-01-13 | 2011-08-24 | Co2 Norway As | Method and plant for handling carbon dioxide from flue gas |
US8043588B2 (en) | 2006-01-13 | 2011-10-25 | Co2-Norway As | Method and plant for removing carbon dioxide from flue gas |
US20100031624A1 (en) * | 2008-07-18 | 2010-02-11 | Siemens Power Generation, Inc. | Fuel heating via exhaust gas extraction |
US8015793B2 (en) | 2008-07-18 | 2011-09-13 | Siemens Energy, Inc. | Fuel heating via exhaust gas extraction |
US8720203B2 (en) | 2010-10-21 | 2014-05-13 | Kabushiki Kaisha Toshiba | Carbon dioxide recovery method and carbon-dioxide-recovery-type steam power generation system |
EP2703607A1 (en) * | 2012-09-04 | 2014-03-05 | Alstom Technology Ltd | A method of increasing electricity output during high demand |
US9617915B2 (en) | 2012-09-04 | 2017-04-11 | General Electric Technology Gmbh | Method of increasing electricity output during high demand |
CN106194300A (en) * | 2016-08-18 | 2016-12-07 | 牛辉英 | A kind of industrial tail gas liquefaction energy-storing and power-generating system and electricity-generating method |
Also Published As
Publication number | Publication date |
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NO20023050L (en) | 2003-12-22 |
CN1671463A (en) | 2005-09-21 |
NO20023050D0 (en) | 2002-06-21 |
RU2315186C2 (en) | 2008-01-20 |
CN1317052C (en) | 2007-05-23 |
RU2005101350A (en) | 2005-08-10 |
AU2003278026A8 (en) | 2004-01-06 |
CA2490429A1 (en) | 2003-12-31 |
JP2006506568A (en) | 2006-02-23 |
EP1539330A2 (en) | 2005-06-15 |
CA2490429C (en) | 2011-04-19 |
JP4885449B2 (en) | 2012-02-29 |
WO2004001301A3 (en) | 2004-02-26 |
AU2003278026A1 (en) | 2004-01-06 |
WO2004001301A2 (en) | 2003-12-31 |
US7328581B2 (en) | 2008-02-12 |
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